Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

In Taiwan, dried Acacia confusa bark is boiled in water to make a decoction traditionally used to treat diarrhoea and dysentery; patients usually drink about 30 ml twice daily after meals (Chiang et al., 2012). Among the indigenous Amis of eastern Taiwan, fresh leaves are crushed into a moist poultice and applied to cuts or insect bites for 15–20 minutes before rinsing (Huang et al., 2017). In the Philippines, the Tagalog community prepares a leaf tea by steeping dried leaves in hot water; the infusion, sweetened with honey, is taken two to three times daily to soothe coughs (Sanchez et al., 2019). Hakka villages in southern Taiwan mash fresh roots with a little warm water to form a paste applied as a poultice to boils and other skin infections, refreshing the dressing twice daily (Wu et al., 2018). These water‑based preparations involve leaves, bark or roots and show how the same species serves diverse therapeutic purposes across three cultural settings.

Leaf tea is made by placing 3 g of dried Acacia confusa leaves (about one heaping teaspoon) into a small teapot, adding 250 ml of freshly boiled water, covering and steeping for 10 minutes. The infusion is strained and served warm; many users add a teaspoon of honey for flavour. The tea is normally drunk twice a day—once in the morning and again after the main meal. Safety notes: pregnant women and children under five should avoid regular use, and people taking anticoagulants or who are sensitive to tannins should limit consumption to one cup daily to prevent mild stomach upset.

Chemical analyses of Acacia confusa have consistently identified flavonoids (quercetin, kaempferol, myricetin) and phenolic acids (gallic and caffeic acids) in both leaves and bark (Lin & Tsai, 2019). The bark also contains high levels of condensed tannins—primarily proanthocyanidins—that impart astringent activity, while the leaves are especially rich in flavonol glycosides. These compounds are well‑documented for antimicrobial, antioxidant and anti‑inflammatory effects, which explain the traditional use of leaf infusions for cough and bark decoctions for diarrhoea.

Recent pharmacological studies show that methanol extracts of Acacia confusa bark inhibit growth of diarrhoea‑causing bacteria such as Escherichia coli, Shigella and Vibrio cholerae, supporting the traditional decoction’s use (Chen et al., 2021). A commercial “Taiwan Acacia Cough Tea” made from standardized leaf material is now sold in health‑food stores, indicating renewed market interest. Ongoing ethnobotanical surveys continue to document these practices among Hakka, Amis and Tagalog communities, and the plant’s well‑characterized flavonoids and tannins make it a candidate for future drug‑discovery projects.

General Uses Top

Suggest a correction!

Common products:
- Timber (sawn lumber) from the heartwood; charcoal.

Industrial and craft applications:
- High-density wood used for construction, flooring, furniture, tool handles, carving, and musical instrument parts; also processed into charcoal and used as fuelwood. Not a commercial source of timber internationally, but widely used domestically/regionally in its native and introduced range.

Properties relevant to use:
- Wood density around 0.75–0.85 g/cm³; yellowish-brown heartwood with fine to medium texture; moderate durability in outdoor use; suitable density and hardness for carving and turned goods; carbonized wood suitable for fuelwood and charcoal due to density.

Sustainability and sourcing:
- Fast-growing, nitrogen-fixing legume used in erosion control, reforestation, and woodlot plantings; supplies are mainly from plantation thinning/maintenance rather than long-rotation commercial forestry; individual or community-scale harvesting typical.

Synonyms Top

Scientific name	Authority	First published in
Racosperma confusum	(Merr.) Pedley	Bot. J. Linn. Soc.92: 248 (1986)
Acacia confusa var. inamuroi	Hayata	Icon. Pl. Formosan.4: 4 (1914)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	small philippine acacia
English	formosa acacia
Persian	آکاکیا کنفوسا
Japanese	ソウシジュ
Japanese	タイワンヤナギ
Japanese	タイワンアカシア
nan	siuⁿ-si-á
pwn	tjuqulj
Russian	Акация смешанная
Vietnamese	keo tương tư
Vietnamese	tương tư thụ
Vietnamese	Đài loan tương tư
Chinese	香絲樹
Chinese	臺灣相思樹
Chinese	臺灣相思
Chinese	台灣相思樹
Chinese	假葉豆
Chinese	相思树
Chinese	相思仔
Chinese	台灣相思
Chinese	台湾相思
Chinese	台湾柳
Chinese	孩儿茶
Chinese	相思樹

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Western Indian Ocean
  - Mauritius
  - Seychelles

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - India
- Indo-China
  - Myanmar
  - Vietnam
- Malesia
  - Borneo
  - Malaya
  - Philippines
  - Sumatera

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
  - Marianas

Southern America click to expand
- Caribbean
  - Dominican Republic

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000186120
USDA Plants	ACCO
Tropicos	13037318
KEW	urn:lsid:ipni.org:names:470039-1
The Plant List	ild-32525
Open Tree Of Life	560305
NCBI Taxonomy	3809
Nature Serve	2.156145
IUCN Red List	18435782
IPNI	470039-1
iNaturalist	47444
GBIF	2978466
Freebase	/m/02qbn3z
EPPO	ACACU
EOL	643764
USDA GRIN	810
Wikipedia	Acacia_confusa
CMAUP	NPO996

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_037074495.1	ASM3707449v1	Chromosome	Agricultural Genomics Institute at Shenzhen, Chinese	2024-03-13	72	537.87 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China

Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S

BMC Ecol Evol

10-Apr-2024

PMCID:	PMC11005248
doi:	10.1186/s12862-024-02227-0
PMID:	38600505

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Copaifera mildbraedii Desf.: Phytochemical Composition of Extracts, Essential Oil, and In Vitro Biological Activities of Bark

Namkona AF, Rahmani R, Worowounga X, Syssa-Magalé JL, Matondo H, Bouajila J

Plants (Basel)

19-Mar-2024

PMCID:	PMC10974413
doi:	10.3390/plants13060877
PMID:	38592880

Flavonoids: A treasure house of prospective pharmacological potentials

Hasnat H, Shompa SA, Islam MM, Alam S, Richi FT, Emon NU, Ashrafi S, Ahmed NU, Chowdhury MN, Fatema N, Hossain MS, Ghosh A, Ahmed F

Heliyon

09-Mar-2024

PMCID:	PMC10944245
doi:	10.1016/j.heliyon.2024.e27533
PMID:	38496846

Melanoxetin: A Hydroxylated Flavonoid Attenuates Oxidative Stress and Modulates Insulin Resistance and Glycation Pathways in an Animal Model of Type 2 Diabetes Mellitus

Rocha S, Amaro A, Ferreira-Junior MD, Proença C, Silva AM, Costa VM, Oliveira S, Fonseca DA, Silva S, Corvo ML, Freitas M, Matafome P, Fernandes E

Pharmaceutics

09-Feb-2024

PMCID:	PMC10892797
doi:	10.3390/pharmaceutics16020261
PMID:	38399315

Biochar as Alternative Material for Heavy Metal Adsorption from Groundwaters: Lab-Scale (Column) Experiment Review

Viotti P, Marzeddu S, Antonucci A, Décima MA, Lovascio P, Tatti F, Boni MR

Materials (Basel)

07-Feb-2024

PMCID:	PMC10890072
doi:	10.3390/ma17040809
PMID:	38399060

Characteristics and Species Diversity of Semi-Natural Plant Communities on Langqi Island

Liu Y, Huang Y, Wang Y, Wang C, Xiao Z, Shen S, Zeng J, Deng C

Biology (Basel)

24-Dec-2023

PMCID:	PMC10813280
doi:	10.3390/biology13010011
PMID:	38248442

Response of leaf functional traits to soil nutrients in the wet and dry seasons in a subtropical forest on an island

Zhang J, Liang M, Tong S, Qiao X, Li B, Yang Q, Chen T, Hu P, Yu S

Front Plant Sci

07-Dec-2023

PMCID:	PMC10748499
doi:	10.3389/fpls.2023.1236607
PMID:	38143586

Damage by typhoon Hato compared among three different plant communities in Macau, China

Yi Q, Ye W, Wang F, Xing F, Harris A, Duan L, Chen H

Ecol Evol

05-Oct-2023

PMCID:	PMC10555504
doi:	10.1002/ece3.10574
PMID:	37809357

Changes in soil organic carbon and nitrogen stocks in organic farming practice and abandoned tea plantation

Juang KW, Chen CP

Bot Stud

28-Sep-2023

PMCID:	PMC10533459
doi:	10.1186/s40529-023-00401-z
PMID:	37759128

Identification of Lasiodiplodia species inciting stem rot of dragon fruit in India through polyphasic approach

Ganesan S, Kumari N, Sahu S, Pattanaik M, Kishore K

3 Biotech

05-Sep-2023

PMCID:	PMC10480115
doi:	10.1007/s13205-023-03754-1
PMID:	37681113

Advances on Cellulose Manufacture in Biphasic Reaction Media

Fernández-Bautista M, Martínez-Gómez S, Rivas S, Alonso JL, Parajó JC

Int J Mol Sci

03-Aug-2023

PMCID:	PMC10418468
doi:	10.3390/ijms241512404
PMID:	37569779

Spatial database of planted forests in East Asia

Abbasi AO, Tang X, Harris NL, Goldman ED, Gamarra JG, Herold M, Kim HS, Luo W, Silva CA, Tchebakova NM, Mitra A, Finegold Y, Jahanshahi MR, Alvarez CI, Kim TK, Ryu D, Liang J

Sci Data

22-Jul-2023

PMCID:	PMC10363164
doi:	10.1038/s41597-023-02383-w
PMID:	37481639

Ultrasound-Assisted Extraction of Verbascoside from Clerodendrum glandulosum Leaves for Analysis of Antioxidant and Antidiabetic Activities

Khound P, Sarma H, Sarma PP, Jana UK, Devi R

ACS Omega

31-May-2023

PMCID:	PMC10268293
doi:	10.1021/acsomega.3c00173
PMID:	37323385

Phylogenomic Analysis of micro-RNA Involved in Juvenile to Flowering-Stage Transition in Photophilic Rice and Its Sister Species

Dash PK, Gupta P, Sreevathsa R, Pradhan SK, Sanjay TD, Mohanty MR, Roul PK, Singh NK, Rai R

Cells

12-May-2023

PMCID:	PMC10216681
doi:	10.3390/cells12101370
PMID:	37408207

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1021/JF050550M
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Isovanillic Acid	12575	Click to see	168.15	unknown	https://doi.org/10.1021/JF050550M
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethyl 3,4-Dihydroxybenzoate	77547	Click to see CCOC(=O)C1=CC(=C(C=C1)O)O	182.17	unknown	https://doi.org/10.1021/JF050550M
Protocatechuic acid, methyl ester	287064	Click to see COC(=O)C1=CC(=C(C=C1)O)O	168.15	unknown	https://doi.org/10.1021/JF050550M
> Benzenoids / Naphthalenes
1,8-Dimethoxynaphthalene	3998082	Click to see	188.22	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
(2R,4S)-4-(4-hydroxy-5-methoxynaphthalen-1-yl)-2-methyl-3,4-dihydro-2H-chromen-5-ol	42605049	Click to see	336.40	unknown	via CMAUP database
8-Methoxynaphthalene-1-ol	10866824	Click to see COC1=CC=CC2=C1C(=CC=C2)O	174.20	unknown	via CMAUP database
Nodulisporin E	42604934	Click to see CC1CC(C2=C(C=CC=C2O1)O)C3=C(C4=C(C=CC=C4OC)C=C3)O	336.40	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Orcinol	10436	Click to see	124.14	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives / 5-unsubstituted pyrrogallols
Pyrogallol	1057	Click to see	126.11	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R,4R,5R)-2,4,6-trimethyloct-6-ene-3,5-diol	42605051	Click to see	186.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol	344467	Click to see	426.70	unknown	https://doi.org/10.1071/CH9670811
Taraxerol	92097	Click to see	426.70	unknown	https://doi.org/10.1071/CH9670811
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1071/CH9670811
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1071/CH9670811
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17S)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	163082001	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1071/CH9670811
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1071/CH9670811
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-Phenylethyl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside	11166301	Click to see	430.40	unknown	via CMAUP database
hydrangeifolin I	10549806	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O	416.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxyphenyl)butan-1-one	4090226	Click to see CCCC(=O)C1=C(C=CC=C1O)O	180.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5-Hydroxy-2-hydroxymethyl-4h-chromen-4-one	42604935	Click to see	192.17	unknown	via CMAUP database
5-hydroxy-2-methyl-4H-chromen-4-one	821390	Click to see	176.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2-Hydroxyvertixanthone	14309394	Click to see COC(=O)C1=C(C=CC2=C1C(=O)C3=C(C=CC=C3O2)O)O	286.24	unknown	via CMAUP database
3,4-dihydroglobosuxanthone A	44598034	Click to see COC(=O)C1(C(CCC2=C1C(=O)C3=C(C=CC=C3O2)O)O)O	306.27	unknown	via CMAUP database
Globosuxanthone A	16046111	Click to see	304.25	unknown	via CMAUP database
Vertixanthone	14309393	Click to see	270.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
N-Methyltryptamine	6088	Click to see CNCCC1=CNC2=CC=CC=C21	174.24	unknown	https://doi.org/10.1002/MRC.1959 https://doi.org/10.1002/JCCS.200000178 https://doi.org/10.1071/CH9670811 https://doi.org/10.2307/4117899
N,N-Dimethyltryptamine	6089	Click to see	188.27	unknown	https://doi.org/10.1002/MRC.1959 https://doi.org/10.1002/JCCS.200000178 https://doi.org/10.1071/CH9670811
> Organoheterocyclic compounds / Lactones / Delta valerolactones
CID 14376452	14376452	Click to see CC=C(C)C1C(C(C(C(=O)O1)(C)C)O)C	212.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid	2518	Click to see	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	https://doi.org/10.1002/JCCS.200000178
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1002/JCCS.200000178
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1002/JCCS.200000178
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
3',4',7,8-Tetrahydroxyflavanone	12309904	Click to see C1C(OC2=C(C1=O)C=CC(=C2O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1021/JF050550M
Isookanin	91196552	Click to see C1C(OC2=C(C1=O)C=CC(=C2O)O)C3=CC(=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1021/JF050550M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,7,8-trihydroxy-2,3-dihydrochromen-4-one	21721859	Click to see	304.25	unknown	https://doi.org/10.1021/JF050550M https://doi.org/10.1002/JCCS.200000178
3,7,8,3',4'-Pentahydroxy flavanone	73829902	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C(=C(C=C3)O)O)O)O)O	304.25	unknown	https://doi.org/10.1021/JF050550M https://doi.org/10.1002/JCCS.200000178
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
(2R,3R,4R)-2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromene-3,4,7,8-tetrol	163019372	Click to see	320.29	unknown	https://doi.org/10.1002/JCCS.200000178 https://doi.org/10.1021/JF102689K
(2R,3R,4R)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol	169996	Click to see	306.27	unknown	https://doi.org/10.1002/JCCS.200000178
(2S,3S,4S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,4,7,8-tetrol	162879389	Click to see	306.27	unknown	https://doi.org/10.1021/JF102689K
2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromene-3,4,7,8-tetrol	163019371	Click to see COC1=C(C=C(C=C1)C2C(C(C3=C(O2)C(=C(C=C3)O)O)O)O)O	320.29	unknown	https://doi.org/10.1021/JF102689K https://doi.org/10.1002/JCCS.200000178
2-(3,4-Dihydroxyphenyl)-3,4,7,8-chromanetetrol	494064	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C(=C(C=C3)O)O)O)O)O)O	306.27	unknown	https://doi.org/10.1002/JCCS.200000178
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,3',4'-Trihydroxyflavone	5322065	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O	270.24	unknown	https://doi.org/10.1021/JF901498Q
7,8,3',4'-Tetrahydroxyflavone	688798	Click to see	286.24	unknown	https://doi.org/10.1021/JF102689K https://doi.org/10.1021/JF901498Q
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,7,8-Trihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one	49835129	Click to see	316.26	unknown	https://doi.org/10.1021/JF050550M https://doi.org/10.1021/JF901498Q
Melanoxetin	15560442	Click to see	302.23	unknown	https://doi.org/10.1021/JF901498Q https://doi.org/10.1021/JF102689K https://doi.org/10.1002/JCCS.200000178 https://doi.org/10.1021/JF050550M
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1021/NP990482W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]-5,7-dihydroxychromen-4-one	25105545	Click to see	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6R)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] 3,4,5-trihydroxybenzoate	44583691	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	616.50	unknown	https://doi.org/10.1021/NP990482W
[(2R,3S,4S,5R,6R)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-5-hydroxy-6-methyl-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate	10795253	Click to see	768.60	unknown	https://doi.org/10.1021/NP990482W
[(2R,3S,4S,5R,6R)-3,5-dihydroxy-2-[5-hydroxy-7-methoxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-6-methyloxan-4-yl] 3,4,5-trihydroxybenzoate	10604042	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	630.50	unknown	https://doi.org/10.1021/NP990482W
[(2R,3S,4S,5S,6R)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate	44583690	Click to see	616.50	unknown	https://doi.org/10.1021/NP990482W
[(2R,3S,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-7-methoxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate	10627784	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	630.50	unknown	https://doi.org/10.1021/NP990482W
[(2S,3S,4R,5R,6S)-4,5-dihydroxy-2-[5-hydroxy-7-methoxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate	163024461	Click to see	630.50	unknown	https://doi.org/10.1021/NP990482W
[(2S,3S,4R,5S,6R)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-5-hydroxy-6-methyl-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate	162894630	Click to see	768.60	unknown	https://doi.org/10.1021/NP990482W
[2-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate	59386481	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	616.50	unknown	https://doi.org/10.1021/NP990482W
[2-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-5-hydroxy-6-methyl-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate	74978316	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O	768.60	unknown	https://doi.org/10.1021/NP990482W
[3,5-Dihydroxy-2-[5-hydroxy-7-methoxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-6-methyloxan-4-yl] 3,4,5-trihydroxybenzoate	85202463	Click to see	630.50	unknown	https://doi.org/10.1021/NP990482W
[4,5-Dihydroxy-2-[5-hydroxy-7-methoxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate	74978408	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O	630.50	unknown	https://doi.org/10.1021/NP990482W
3-O-Galloylmucic acid	74978303	Click to see	616.50	unknown	https://doi.org/10.1021/NP990482W
3'-O-methyltricetin 3-O-alpha-L-rhamnopyranoside	72551450	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)OC)O)O)O)O)O	478.40	unknown	via CMAUP database
5-Hydroxy-7-methoxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	74978406	Click to see	478.40	unknown	https://doi.org/10.1021/NP990482W
5-hydroxy-7-methoxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	163086215	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC(=C(C(=C4)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1021/NP990482W
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One	5352000	Click to see	464.40	unknown	https://doi.org/10.1021/NP990482W
5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	9890615	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP990482W
Quercitrin	5280459	Click to see	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Fisetin 3-methyl ether	9839293	Click to see	300.26	unknown	https://doi.org/10.1021/JF901498Q
Transilitin	44258702	Click to see	316.26	unknown	https://doi.org/10.1021/JF901498Q https://doi.org/10.1021/JF050550M
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
7,8,3'-Trihydroxy-3,4'-dimethoxyflavone	24813969	Click to see	330.29	unknown	https://doi.org/10.1021/JF901498Q
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',3',4',3,4-Pentahydroxychalcone	261164	Click to see	288.25	unknown	https://doi.org/10.1021/JF102689K https://doi.org/10.1021/JF050550M https://doi.org/10.1021/JF901498Q
Okanin	5281294	Click to see	288.25	unknown	https://doi.org/10.1021/JF102689K https://doi.org/10.1021/JF901498Q https://doi.org/10.1021/JF050550M

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Acacia confusa

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top